CN114506838B - Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof - Google Patents
Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof Download PDFInfo
- Publication number
- CN114506838B CN114506838B CN202210144670.5A CN202210144670A CN114506838B CN 114506838 B CN114506838 B CN 114506838B CN 202210144670 A CN202210144670 A CN 202210144670A CN 114506838 B CN114506838 B CN 114506838B
- Authority
- CN
- China
- Prior art keywords
- carbon aerogel
- aerogel material
- dimensional
- conductive network
- precursor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/05—Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0091—Preparation of aerogels, e.g. xerogels
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
The invention discloses a three-dimensional conductive network reinforced nickel-doped carbon aerogel material, a preparation method and application thereof, wherein a three-dimensional conductive network precursor is treated for standby; emulsifying the glucose solution and the molten paraffin to obtain an oil-in-water emulsion, adding a three-dimensional conductive network precursor, nickel hydroxide, acrylamide, methylene bisacrylamide and ammonium persulfate, and freeze-drying to obtain a carbon aerogel material precursor at 300-600 ℃; and mixing and evaporating the carbon aerogel material precursor and the potassium hydroxide solution to dryness, and carbonizing the mixture at a high temperature of between 700 and 900 ℃ to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material. According to the invention, the first-dimension biological carbon and the second-dimension biological carbon and the metallic nickel are doped in situ in the carbon aerogel material together to form a three-dimensional conductive network structure together, so that the mechanical strength of the carbon aerogel material is improved, the conductivity of the carbon aerogel material is improved, and the electrochemical performance of the carbon aerogel material is further improved.
Description
Technical Field
The invention belongs to the technical field of carbon materials, and particularly relates to a three-dimensional conductive network reinforced nickel-doped carbon aerogel material, and a preparation method and application thereof.
Background
The carbon aerogel material is a novel carbon material, and has rich nanoscale pore diameter and high specific surface area (600-1100 m 2 And/g), high conductivity, stable physical and chemical properties, controllable structure, easy doping and the like, and is widely applied to the fields of adsorption, energy storage, conversion, heat insulation, aerospace and the like.
Since the discovery of aerogels from the beginning of the 30 s of the 20 th century, a variety of ultra-light porous materials have been prepared, such as silica aerogel, metal foam, CNT aerogel, etc., and carbon aerogel materials are considered ideal energy storage materials, catalysts, catalyst supports, chemisorbers, thermal insulators, soundproofing materials, etc. because of their advantages of controllable pore size, low density, good electrical conductivity, low thermal conductivity, etc.
Because of its unique pore structure and its properties, carbon aerogel materials have been one of the popular fields of research in recent years, particularly in the field of lithium secondary batteries, and some applications and advances have been made in recent years. Such as: (1) The carbon aerogel material and the composite material thereof can be used as a carrier of an electrocatalyst in a battery or can be directly used as a catalyst in an electrochemical process, and because of the special structure of the carbon aerogel material and the composite material thereof, metal particles can be uniformly dispersed, the electrochemical effective surface area, the catalytic activity and the performance of a fuel cell of the catalyst are improved, and meanwhile, the application of the carbon aerogel material and the composite material can reduce the cost and improve the utilization rate and the catalytic activity of the catalyst. (2) The carbon aerogel material can be directly used as an electrode material of a lithium sulfur battery, has higher conductivity, and meanwhile, holes are rich, the specific surface area is large, so that sulfur of the lithium sulfur battery in the charge and discharge process is not easy to dissolve, and the cycle performance of the battery is improved. (3) The carbon aerogel material has the characteristic of easy compounding, can be further doped with the carbon material, and the carbon particles can further enrich the internal structure of the carbon aerogel material while improving the conductivity and the physical strength of the carbon aerogel material, so that a conductive frame is formed, and the electrochemical performance of the material is improved.
Although carbon aerogel materials possess many advantages, their structure and performance can be further improved when used in certain specific applications. When the carbon aerogel is used as an electrode material, particularly as an electrode material of a lithium sulfur battery, the inherent problem of large pore diameter of the carbon aerogel still can influence the adsorption of polysulfide when the carbon aerogel is used as an electrode material carrier of the battery such as the lithium sulfur battery, and the performance stability of the lithium sulfur battery at high cycle can not be ensured. Secondly the conductivity of the carbon aerogel material itself also plays a decisive role in the cycle performance of the cell. In addition, the carbon aerogel itself is mainly physically adsorbed, and has weak chemical adsorption effect on polysulfide, so that it is difficult to effectively ensure the cycle stability of the sulfur anode. In addition, the traditional manufacturing method of the carbon aerogel material is complex, and toxic aldehyde substances are used in the manufacturing process, so that the preparation method of the carbon aerogel material is further improved, the performance of the carbon aerogel material is improved, and the application expansion of the carbon aerogel material in the fields of batteries and the like is particularly important.
Disclosure of Invention
Aiming at the problems of complex manufacturing process, small specific surface area, poor conductivity and no chemical adsorption effect on polysulfide in the existing carbon aerogel material, the invention aims to provide the three-dimensional conductive network reinforced nickel-doped carbon aerogel material, and the preparation method and application thereof.
In order to achieve the above purpose, the present invention adopts the following technical scheme:
the preparation method of the three-dimensional conductive network reinforced nickel-doped carbon aerogel material comprises the following steps:
(1) Washing the three-dimensional conductive network biomass precursor with water, pickling, washing with water, and drying for later use;
(2) Uniformly mixing glucose aqueous solution and molten paraffin, emulsifying to obtain an oil-in-water emulsion, adding the three-dimensional conductive network biomass precursor prepared in the step (1), adding nickel hydroxide, acrylamide, methylene bisacrylamide and ammonium persulfate to obtain a composite hydrogel, and performing pre-carbonization at 300-600 ℃ after freeze drying to obtain a carbon aerogel material precursor;
(3) Uniformly mixing the carbon aerogel material precursor obtained in the step (2) with a potassium hydroxide solution, evaporating to dryness, and carbonizing at a high temperature of 700-900 ℃ to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Preferably, in the step (1), the three-dimensional conductive network biomass precursor includes a one-dimensional biochar-based precursor and a two-dimensional biochar-based precursor; the one-dimensional biochar-based precursor is selected from at least one of absorbent cotton, phoenix tree wadding and cattail wool; the two-dimensional biochar-based precursor is selected from at least one of peanut shells, hibiscus flower petals and magnolia flower petals.
More preferably, the mass ratio of the one-dimensional biochar-based precursor to the two-dimensional biochar-based precursor is 1:1 to 3.
Preferably, in the step (1), the three-dimensional conductive network biomass precursor is firstly washed by deionized water, then soaked in 30-35 wt% hydrochloric acid or 10-30 wt% nitric acid for 8-12 hours, then washed to be neutral by ionized water, and finally dried at 60-100 ℃ for standby.
Preferably, in step (2), the step of preparing the composition comprises the steps of: paraffin=3 to 5:1, uniformly mixing at 70 ℃, wherein the addition of the biomass precursor of the three-dimensional conductive network is 10-50 wt% of glucose, and the addition of nickel hydroxide is 0.8-2.0 wt% of paraffin; the mass ratio of the acrylamide to the methylene bisacrylamide to the ammonium persulfate to the glucose is 9:1:2:30.
preferably, in step (3), the method comprises the steps of: carbon aerogel material precursor = 2-5: 1 is immersed for 12 hours at the temperature of 100-150 ℃, then carbonized for 2-4 hours at the high temperature of 700-900 ℃, and then washed with dilute hydrochloric acid and water until neutral, thus obtaining the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
The invention also provides the three-dimensional conductive network reinforced nickel-doped carbon aerogel material prepared by the preparation method.
The invention also provides application of the three-dimensional conductive network reinforced nickel-doped carbon aerogel material in preparing a lithium-sulfur battery positive electrode material.
The inventor finds that the dimension of one-dimensional biochar (such as carbon micro-tubes and carbon fiber materials) is small, the mutual contact between the carbon micro-tubes or the carbon fiber materials is less, the effective transmission of electrons in the whole linear network is not facilitated, the one-dimensional biochar (such as carbon micro-tubes and carbon fiber materials) and the two-dimensional biochar (such as graphene-like materials) are commonly and in-situ doped in the carbon aerogel materials, after the two-dimensional biochar materials are added, the physical contact between the one-dimensional biochar and the two-dimensional biochar (the graphene-like materials) is effectively enhanced, a three-dimensional space conductive network with good contact is formed, and the doped nickel has good conductivity, so that the conductivity of the whole composite material is cooperatively improved, and meanwhile, the mechanical property of the carbon aerogel materials can be improved based on the excellent mechanical property of the carbon materials (the one-dimensional biochar and the two-dimensional biochar).
The one-dimensional biochar and the two-dimensional biochar formed in the invention can form a large number of hydrophilic groups on the surface after being subjected to acid treatment in the early stage, so that the hydrophilic groups are tightly combined with the prepared hydrogel, the interface between the one-dimensional and two-dimensional biochar materials and the carbon aerogel in the carbonization process can be effectively weakened, and the transfer of electrons and ions in the carbon wall is facilitated. In addition, the carbon aerogel prepared by adopting glucose as a carbon source is hard carbon, and has poor conductivity. The first-dimensional precursor material and the second-dimensional precursor material can be effectively graphitized in the carbonization process, and meanwhile, metal nickel with good conductivity is doped, so that the conductivity of the carbon aerogel material is synergistically improved.
In the invention, nickel is doped while one-dimensional biochar and two-dimensional biochar are co-doped in situ. Firstly, nickel metal has good catalytic performance as transition metal, is beneficial to accelerating the reaction kinetics of the carbon aerogel material when being used as the positive electrode of the lithium-sulfur battery, and reduces the loss of active substances of the lithium-sulfur battery; secondly, the nickel metal has good self-conductivity, and after being doped into the carbon aerogel material, the nickel metal can cooperate with a three-dimensional conductive network formed by one-dimensional biochar and two-dimensional biochar to improve the conductivity of the carbon aerogel material; and thirdly, the nickel metal has strong chemical adsorption effect, chemical adsorption effect of chemical bonds formed by the nickel metal on polysulfide in the lithium-sulfur battery is utilized, and the electrochemical performance of the lithium-sulfur battery can be further improved by cooperating with physical adsorption effect of the carbon aerogel material.
The invention relates to a three-dimensional conductive network reinforced nickel-doped carbon aerogel material, which is realized by the steps of firstly emulsifying a water phase taking glucose as a raw material and an oil phase taking paraffin as a raw material, adding a gel and a catalyst to form hydrogel, freeze-drying to obtain an organic aerogel, pre-carbonizing at 300-600 ℃ to remove the oil phase, finally adding potassium hydroxide to perform heat preservation and pore forming treatment at 700-900 ℃, and forming a large number of micropores on the carbon wall of the carbon aerogel, so that the carbon wall can be thinned on one hand, and conductive particle transmission is facilitated; on the other hand, for lithium sulfur batteries, these micropores can effectively store sulfur and polysulfide and effectively adsorb them, thereby improving the cycling stability of the sulfur positive electrode.
When the carbon aerogel material prepared by the invention is used as a lithium sulfur battery anode modified material:
1. the specific surface area of the carbon aerogel material is large, and simultaneously the doped active carbon materials (one-dimensional biochar and two-dimensional biochar) and nickel metal can form a conductive framework in the carbon aerogel material, so that the volume expansion of active substances of the lithium-sulfur battery in the reaction process can be accommodated;
2. the carbon aerogel material has a catalytic effect, the catalytic performance is further enhanced after the transition metal nickel with the catalytic performance is doped, the reaction speed of the lithium-sulfur battery in the shuttle effect in the charge and discharge process can be accelerated, and the loss of active substances is reduced;
3. the doped active carbon material has a large number of oxygen-containing functional groups, and the invention utilizes the polar adsorption effect of the oxygen-containing functional groups on polysulfide in the lithium sulfur battery to improve the performance of the lithium sulfur battery;
4. the doped nickel metal has strong chemical adsorption effect, and the invention utilizes the chemical adsorption effect of the nickel metal forming chemical bond to polysulfide in the lithium sulfur battery to improve the performance of the lithium sulfur battery.
Based on the reasons, the lithium sulfur battery prepared by the invention has excellent cycle performance and specific capacity, and is expected to be widely applied to the field of lithium sulfur batteries.
According to the invention, glucose and paraffin are used as raw materials, a carbon aerogel material prepared by a trans-emulsion polymerization method is used as a carrier, and a one-dimensional biological carbon-based precursor, a two-dimensional biological carbon-based precursor and nickel metal are doped to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material. According to the preparation method, the biochar precursors are not required to be carbonized and then added into the hydrogel, so that the influence on a large amount of loss and impurities in the carbonization process of the first-dimension and second-dimension biochar precursor materials is reduced, and the interface effect between the formed first-dimension and second-dimension biochar materials and the carbon aerogel is also weakened. The doped one-dimensional and two-dimensional biological carbon material and nickel metal not only can improve the conductivity of the carbon aerogel material, but also can improve the adsorption performance and the catalytic performance, the carbon material also forms various structures in the carbon aerogel material, and the conductive framework is formed while the mechanical strength of the material is improved, so that the service performance of the carbon aerogel material is greatly improved.
Compared with the prior art, the invention has the advantages that:
(1) According to the three-dimensional conductive network reinforced nickel-doped carbon aerogel material, one-dimensional biological carbon (such as a carbon micron tube and a carbon fiber material) and two-dimensional biological carbon (such as a graphene material) are commonly and in-situ doped to form a three-dimensional conductive network, so that the mechanical strength of the carbon aerogel material can be improved, the conductivity of the carbon aerogel material can be improved, and the electrochemical performance, the adsorption performance and the catalytic performance of the carbon aerogel material can be further improved.
(2) The three-dimensional conductive network reinforced nickel-doped carbon aerogel material is doped with the nickel metal material, so that the conductivity and catalytic performance of the material can be improved, and meanwhile, the chemical adsorption effect can be provided, and the electrochemical performance and adsorption performance of the material are further improved.
(3) The three-dimensional conductive network reinforced nickel-doped carbon aerogel material provided by the invention has the advantages that micropores are taken as a main material, mesopores are taken as an auxiliary material, a large number of micron-sized holes are distributed on the surface of particles, the porous rate and the specific surface area are extremely high, the adsorption of polysulfide is facilitated, and meanwhile, the effect of relieving the volume expansion of the electrode material which is inevitably generated can be achieved, so that the cycle performance of a battery is improved.
Drawings
FIG. 1 is a graph of the impedance of a three-dimensional conductive network-reinforced nickel-doped carbon aerogel material prepared in example 3;
FIG. 2 is an XRD pattern of the three-dimensional conductive network enhanced nickel doped carbon aerogel material prepared in example 3, wherein Ca represents the three-dimensional conductive network enhanced undoped nickel carbon aerogel material and Ca/Ni represents the three-dimensional conductive network enhanced nickel doped carbon aerogel material.
Detailed Description
The following examples are intended to further illustrate the invention without limiting it.
Example 1
(1) Washing Firmiana tree seed and ground peanut shell with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10 hr, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 1g of phoenix tree cotton and 2g of peanut shells treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylenebisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cutting the milky hydrogel into small pieces with the thickness of 1-3 mu m after the milky hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the frozen and dried sample into a porcelain boat, and keeping the temperature in a nitrogen atmosphere for 2h at a speed of 5 ℃/min from room temperature to 400 ℃ by using a tubular furnace to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acid after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Example 2
(1) Washing absorbent cotton and ground peanut shells with deionized water for 3 times, respectively soaking in 30wt% hydrochloric acid for 10 hours, washing with ionized water to neutrality, and drying at 80deg.C for use;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 1g of absorbent cotton and 2g of peanut shells treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (4.5 g of acrylamide and 0.5g of methylene bisacrylamide) and a catalyst (1 g of ammonium persulfate), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cutting the hydrogel into small sheets with the thickness of 1-3 mu m after the hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the frozen and dried sample into a porcelain boat, and keeping the temperature at 5 ℃/min to 400 ℃ in a nitrogen atmosphere for 2h by using a tubular furnace to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acid after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Example 3
(1) Washing Firmiana tree cotton, absorbent cotton and ground peanut shells with deionized water for 3 times, respectively soaking in 30wt% hydrochloric acid for 10 hours, washing with ionized water to neutrality, and drying at 80deg.C for use;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a 70 ℃ water bath to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, adding 1g of phoenix tree cotton, 1g of peanut shell and 1g of absorbent cotton treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylene bisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing milky hydrogel, preserving heat at 70 ℃ for 30min, taking out, cutting the milky hydrogel into small pieces with the thickness of 1-3 mu m after the milky hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the freeze-dried sample into a porcelain boat, heating up at a speed of 5 ℃/min to 400 ℃ from room temperature by a tubular furnace, and preserving heat in nitrogen atmosphere for 2h to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acid after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Example 4
(1) Washing Firmiana tree cotton, absorbent cotton and ground peanut shells with deionized water for 3 times, respectively soaking in 30wt% hydrochloric acid for 10 hours, washing with ionized water to neutrality, and drying at 80deg.C for use;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a 70 ℃ water bath to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 1.25g of phoenix tree wadding, 1.25g of peanut shell and 5g of absorbent cotton treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (4.5 g of acrylamide and 0.5g of methylene bisacrylamide) and a catalyst (1 g of ammonium persulfate), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cutting the hydrogel into small sheets with the thickness of 1-3 mu m after the hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the freeze-dried sample into a porcelain boat, heating the sample from room temperature to 400 ℃ at a speed of 5 ℃/min in a tube furnace, and keeping the temperature for 2h in nitrogen atmosphere to obtain a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acid after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Example 5
(1) Washing Firmiana tree seed and ground peanut shell with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10 hr, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, adding 1g of phoenix tree wadding and 2g of peanut shells treated in the step (1), adding 0.04g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylenebisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cutting the milky hydrogel into small pieces with the thickness of 1-3 mu m after the milky hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the frozen and dried sample into a porcelain boat, and keeping the temperature in a nitrogen atmosphere for 2h at a speed of 5 ℃/min from room temperature to 400 ℃ by using a tubular furnace to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acid after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
Comparative example 1
(1) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80) and heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, adding 0.05g of nickel hydroxide, then ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (4.5 g of acrylamide and 0.5g of methylene bisacrylamide) and a catalyst (1 g of ammonium persulfate) to obtain milky hydrogel, insulating at 70 ℃ for 30min, taking out, cooling to room temperature, cutting into small flakes with the thickness of 1-3 mu m, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the freeze-dried sample into a porcelain boat, heating up to 400 ℃ from room temperature by a tubular furnace at the speed of 5 ℃/min, and insulating in a nitrogen atmosphere for 2h to obtain a carbon aerogel material precursor;
(2) Putting the carbon aerogel material precursor prepared in the step (1) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, washing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acidic after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the nickel-doped carbon aerogel material.
Comparative example 2
(1) Washing Firmiana tree seed with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10h, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 3g of phoenix tree wadding treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylenebisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing a milky white hydrogel, preserving heat at 70 ℃ for 30min, taking out, cutting the milky white hydrogel into small flakes with the thickness of 1-3 mu m after the milky white hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the frozen and dried sample into a porcelain boat, and heating from room temperature to 400 ℃ in a nitrogen atmosphere at a speed of 5 ℃/min by using a tube furnace to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acidic after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the one-dimensional biochar-enhanced nickel-doped carbon aerogel material.
Comparative example 3
(1) Washing ground peanut shells with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10 hours, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 3g of ground peanut shells treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylenebisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cooling to room temperature, cutting into small flakes with the thickness of 1-3 mu m, freezing at-55 ℃ for 12h, vacuum drying for 48h, putting the freeze-dried sample into a porcelain boat, and heating from room temperature to 400 ℃ at a speed of 5 ℃/min in a tubular furnace, keeping the temperature for 2h in a nitrogen atmosphere to obtain a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acidic after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and then placing the mixture into a baking oven at 60 ℃ for drying to obtain the two-dimensional biochar-enhanced nickel-doped carbon aerogel material.
Comparative example 4
(1) Washing absorbent cotton with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10h, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 3g of absorbent cotton treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylenebisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing milky hydrogel, keeping the temperature at 70 ℃ for 30min, taking out, cutting the milky hydrogel into small flakes with the thickness of 1-3 mu m after the milky hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the freeze-dried sample into a porcelain boat, and heating from room temperature to 400 ℃ at a speed of 5 ℃/min in a nitrogen atmosphere by using a tube furnace to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acidic after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the one-dimensional biochar-enhanced nickel-doped carbon aerogel material.
Comparative example 5
(1) Washing Firmiana tree cotton and absorbent cotton with deionized water for 3 times, soaking in 30wt% hydrochloric acid for 10h, washing with ionized water to neutrality, and drying at 80deg.C;
(2) Taking 4g of paraffin and 0.56g of span 80 (span-80), and heating in a water bath kettle at 70 ℃ until the paraffin is completely dissolved into colorless transparent liquid to obtain molten paraffin; uniformly stirring 15g of glucose, 23.5ml of deionized water and 1.44g of Tween 80 (Tween-80), heating in a water bath kettle at 70 ℃ to obtain a glucose aqueous solution, slowly adding the glucose aqueous solution into molten paraffin, uniformly stirring, respectively adding 1.5g of phoenix tree wadding and 1.5g of absorbent cotton treated in the step (1), adding 0.05g of nickel hydroxide, ultrasonically stirring at 70 ℃ for 1h, adding a gelling agent (acrylamide 4.5g and methylene bisacrylamide 0.5 g) and a catalyst (ammonium persulfate 1 g), preparing a milky hydrogel, preserving heat at 70 ℃ for 30min, taking out, cutting the milky hydrogel into small flakes with the thickness of 1-3 mu m after the milky hydrogel is cooled to room temperature, freezing at-55 ℃ for 12h, vacuum drying for 48h, placing the frozen and dried sample into a porcelain boat, heating up to 400 ℃ at the speed of 5 ℃/min from room temperature by a tubular furnace, and preserving heat in a nitrogen atmosphere for 2h to prepare a carbon aerogel material precursor;
(3) Putting the carbon aerogel material precursor prepared in the step (2) into a culture dish, and according to the carbon aerogel material precursor: the mass ratio of potassium hydroxide is 1:3 adding potassium hydroxide in proportion, adding a certain amount of deionized water until the potassium hydroxide is completely dissolved, placing the mixture into a baking oven at 100 ℃ for heat preservation for 12 hours, scraping the potassium hydroxide and the carbon aerogel material into a porcelain boat together, starting at room temperature, keeping the temperature at a heating rate of 5 ℃/min until 800 ℃ for 3 hours in a nitrogen atmosphere, flushing the mixture with an excessive 3mol/L dilute hydrochloric acid solution until the sample is weak acidic after the sample is cooled to room temperature, carrying out suction filtration with deionized water until the sample is neutral, and placing the mixture into a baking oven at 60 ℃ for drying to obtain the one-dimensional biochar-enhanced nickel-doped carbon aerogel material.
Preparation of a positive electrode material of a lithium-sulfur battery:
samples prepared in examples 1-4 and comparative examples 1-5 and nano sulfur were taken respectively according to the carbon aerogel materials: the mass ratio of the nano sulfur is 3:7, grinding the mixture in a mortar, uniformly mixing the mixture, collecting the mixture into a reaction kettle, vacuumizing the reaction kettle, preserving the heat of the reaction kettle at 155 ℃ for 12 hours, and then mixing the product with a conductive agent (SuperP) and PVDF according to the following formula 7:2:1, mixing and transferring the mixture into a mortar to be ground uniformly, taking N-methyl pyrrolidone (NMP) as a dispersing agent, mixing the mixture together and transferring the mixture onto a magnetic stirrer to be stirred for 10 hours, flatly coating the mixed slurry on a carbon-coated aluminum foil on a coating machine, setting the coating height of a scraper to be 200 mu m, and finally drying the mixture at a constant temperature of 60 ℃ by using a vacuum drying box to obtain the required lithium sulfur battery anode material, wherein the performances of the required lithium sulfur battery anode material are shown in tables 1-3.
TABLE 1 Main relevant parameter Table for samples prepared in examples 1 to 4 and comparative examples 1 to 5
As shown in Table 1, the samples prepared in examples 1 to 4 and comparative examples 1 to 5 all have higher specific surface areas, and the present invention adopts the mode of in-situ co-doping of one-dimensional biochar and two-dimensional biochar to form a three-dimensional conductive network, which is larger than that of undoped and singly doped comparative examples 1 to 5.
The samples prepared in examples 1 to 4 and comparative examples 1 to 5 were cut into uniform-sized pole pieces using a cutter for use.
And assembling the prepared pole piece, battery shell, lithium piece, diaphragm electrolyte, gasket and shrapnel into a battery in a glove box in argon atmosphere. The separator used in the battery assembly was a polyolefin porous film having a high strength and a thin film, the electrolyte was a solution prepared by dissolving 1MLiTFSI in DOL: dme=1:1v and adding 2% lithium nitrate, and the separator was charged and discharged at a rate of 0.5C at 20 ℃ in a range of 1.7 to 2.8V, and the specific capacity after 100 times of charging and discharging was recorded, and the results are shown in table 2.
Table 2 the cycle properties of the samples prepared in examples 1 to 4 and comparative examples 1 to 5 are shown
As shown in table 2, the three-dimensional conductive network reinforced nickel-doped carbon aerogel material suppresses the shuttle effect and the volume expansion inherent in the lithium-sulfur battery to a certain extent, improves the cycle performance of the battery, and the cycle performance of the mode of forming the three-dimensional conductive network by one-dimensional and two-dimensional co-doping of examples 1 to 4 is obviously improved compared with the mode of single one-dimensional or two-dimensional doping of comparative examples 1 to 5.
Four-probe resistance tests were performed on examples 1 to 4 and comparative examples 1 to 5, and the results are shown in Table 3 below.
Table 3 four-probe resistance test results tables for the samples prepared in examples 1 to 4 and comparative examples 1 to 5
As shown in Table 3, the three-dimensional conductive network reinforced nickel-doped carbon aerogel material of the invention has very excellent conductivity, and compared with the single one-dimensional or two-dimensional doped comparative examples 1 to 5, the three-dimensional conductive network formed by co-doping one of the three-dimensional conductive network and the two-dimensional conductive network in examples 1 to 4 has lower resistance, the conductivity can be obviously improved.
Claims (7)
1. The preparation method of the three-dimensional conductive network reinforced nickel-doped carbon aerogel material is characterized by comprising the following steps of:
(1) Washing the three-dimensional conductive network biomass precursor with water, pickling, washing with water, and drying for later use; the three-dimensional conductive network biomass precursor comprises a one-dimensional biochar-based precursor and a two-dimensional biochar-based precursor; the one-dimensional biochar-based precursor is selected from at least one of absorbent cotton, phoenix tree wadding and cattail wool; the two-dimensional biochar-based precursor is selected from at least one of peanut shells, hibiscus flower petals and magnolia flower petals;
(2) Uniformly mixing a glucose aqueous solution and molten paraffin, emulsifying to obtain an oil-in-water emulsion, adding the three-dimensional conductive network biomass precursor prepared in the step (1), adding nickel hydroxide, acrylamide, methylene bisacrylamide and ammonium persulfate to obtain a composite hydrogel, and performing pre-carbonization at 300-600 ℃ after freeze drying to obtain a carbon aerogel material precursor;
(3) And (3) uniformly mixing the carbon aerogel material precursor obtained in the step (2) with a potassium hydroxide solution, evaporating to dryness, and carbonizing at a high temperature of 700-900 ℃ to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
2. The method of manufacturing according to claim 1, characterized in that: the mass ratio of the one-dimensional biochar-based precursor to the two-dimensional biochar-based precursor is 1: 1-3.
3. The method of manufacturing according to claim 1, characterized in that: in the step (1), the three-dimensional conductive network biomass precursor is firstly washed by deionized water, then soaked in 30-35wt% hydrochloric acid or 10-30wt% nitric acid for 8-12 hours, then washed to be neutral by ionized water, and finally dried at 60-100 ℃ for standby.
4. The method of manufacturing according to claim 1, characterized in that: in the step (2), the following steps are carried out according to glucose: paraffin=3 to 5:1, uniformly mixing at 70 ℃, wherein the addition amount of the biomass precursor of the three-dimensional conductive network is 10-50 wt% of glucose, and the addition amount of nickel hydroxide is 0.8-2.0 wt% of paraffin; the mass ratio of the acrylamide to the methylene bisacrylamide to the ammonium persulfate to the glucose is 9:1:2:30.
5. the method of manufacturing according to claim 1, characterized in that: in the step (3), the following steps are carried out according to potassium hydroxide: carbon aerogel material precursor = 2-5: 1, soaking the nickel-doped carbon aerogel material at the mass ratio of 100-150 ℃ for 12-h, carbonizing the nickel-doped carbon aerogel material at the high temperature of 700-900 ℃ for 2-4 hours, and then carrying out dilute hydrochloric acid washing and water washing to neutrality to obtain the three-dimensional conductive network reinforced nickel-doped carbon aerogel material.
6. The three-dimensional conductive network reinforced nickel-doped carbon aerogel material prepared by the method of any of claims 1-5.
7. The use of a three-dimensional conductive network reinforced nickel doped carbon aerogel material according to claim 6, wherein: it is used for preparing the positive electrode material of the lithium-sulfur battery.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202210144670.5A CN114506838B (en) | 2022-02-17 | 2022-02-17 | Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202210144670.5A CN114506838B (en) | 2022-02-17 | 2022-02-17 | Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN114506838A CN114506838A (en) | 2022-05-17 |
| CN114506838B true CN114506838B (en) | 2023-09-26 |
Family
ID=81552231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202210144670.5A Active CN114506838B (en) | 2022-02-17 | 2022-02-17 | Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN114506838B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117023558B (en) * | 2023-08-18 | 2024-05-24 | 东北石油大学 | Controllable preparation method and application of high-strength biomass glycosyl carbon aerogel material |
| CN117878295B (en) * | 2024-03-12 | 2024-06-07 | 河北省科学院能源研究所 | Composite positive electrode active material, and preparation method and application thereof |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105110313A (en) * | 2015-07-25 | 2015-12-02 | 复旦大学 | Polyimide-based composite carbon aerogel and preparation method therefor |
| WO2017139984A1 (en) * | 2016-02-19 | 2017-08-24 | 肖丽芳 | Preparation method for sulfur doped lithium-sulfur battery cathode material with three-dimensional structure |
| CN110950316A (en) * | 2019-12-13 | 2020-04-03 | 湘潭大学 | High-specific-surface-area multi-element-doped carbon micro-tube-carbon aerogel and preparation method thereof |
| CN111333068A (en) * | 2020-02-28 | 2020-06-26 | 西南大学 | Preparation method and application of biomass porous carbon material based on nut shells |
| CN111740091A (en) * | 2020-07-08 | 2020-10-02 | 中国科学院山西煤炭化学研究所 | Carbon aerogel @ sulfur composite material for lithium-sulfur battery positive electrode and preparation method thereof |
| CN112010291A (en) * | 2020-09-03 | 2020-12-01 | 郑州工程技术学院 | Preparation method and application of nickel-doped molybdenum disulfide/graphene three-dimensional composite material |
| CN112038635A (en) * | 2020-08-04 | 2020-12-04 | 湘潭大学 | Lithium-sulfur battery graphene-loaded cementite particle composite positive electrode material and preparation method thereof |
| CN112142034A (en) * | 2020-09-27 | 2020-12-29 | 武汉理工大学 | Preparation method of sulfur/carbon aerogel composite material |
| CN112279235A (en) * | 2020-09-25 | 2021-01-29 | 湘潭大学 | Metal-doped three-dimensional framework structure graded porous biochar and preparation method thereof |
| CN113035578A (en) * | 2021-03-03 | 2021-06-25 | 武汉理工大学 | Graphene/carbon aerogel composite material and preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018112092A1 (en) * | 2016-12-13 | 2018-06-21 | Domtar Paper Company, Llc | Production of aerogels and carbon aerogels from lignin |
-
2022
- 2022-02-17 CN CN202210144670.5A patent/CN114506838B/en active Active
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105110313A (en) * | 2015-07-25 | 2015-12-02 | 复旦大学 | Polyimide-based composite carbon aerogel and preparation method therefor |
| WO2017139984A1 (en) * | 2016-02-19 | 2017-08-24 | 肖丽芳 | Preparation method for sulfur doped lithium-sulfur battery cathode material with three-dimensional structure |
| CN110950316A (en) * | 2019-12-13 | 2020-04-03 | 湘潭大学 | High-specific-surface-area multi-element-doped carbon micro-tube-carbon aerogel and preparation method thereof |
| CN111333068A (en) * | 2020-02-28 | 2020-06-26 | 西南大学 | Preparation method and application of biomass porous carbon material based on nut shells |
| CN111740091A (en) * | 2020-07-08 | 2020-10-02 | 中国科学院山西煤炭化学研究所 | Carbon aerogel @ sulfur composite material for lithium-sulfur battery positive electrode and preparation method thereof |
| CN112038635A (en) * | 2020-08-04 | 2020-12-04 | 湘潭大学 | Lithium-sulfur battery graphene-loaded cementite particle composite positive electrode material and preparation method thereof |
| CN112010291A (en) * | 2020-09-03 | 2020-12-01 | 郑州工程技术学院 | Preparation method and application of nickel-doped molybdenum disulfide/graphene three-dimensional composite material |
| CN112279235A (en) * | 2020-09-25 | 2021-01-29 | 湘潭大学 | Metal-doped three-dimensional framework structure graded porous biochar and preparation method thereof |
| CN112142034A (en) * | 2020-09-27 | 2020-12-29 | 武汉理工大学 | Preparation method of sulfur/carbon aerogel composite material |
| CN113035578A (en) * | 2021-03-03 | 2021-06-25 | 武汉理工大学 | Graphene/carbon aerogel composite material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN114506838A (en) | 2022-05-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN108529587B (en) | Preparation method and application of phosphorus-doped biomass graded porous carbon material | |
| CN113044827B (en) | Nano carbon material composite biomass hard carbon electrode material and preparation method and application thereof | |
| CN114506838B (en) | Three-dimensional conductive network reinforced nickel-doped carbon aerogel material and preparation method and application thereof | |
| CN109081340B (en) | Pine-based biomass activated carbon, preparation method thereof and application thereof in electrochemical energy storage | |
| CN107244664B (en) | Preparation method and application of graphene-like structure carbon electrode material | |
| CN113247887A (en) | Preparation method of hierarchical porous graphene and application of hierarchical porous graphene | |
| CN110950316A (en) | High-specific-surface-area multi-element-doped carbon micro-tube-carbon aerogel and preparation method thereof | |
| CN112850708A (en) | Preparation method and application of nitrogen-doped porous carbon material with high specific surface area | |
| CN112374485A (en) | Preparation method of nitrogen-phosphorus double-doped foamy carbon for zinc ion hybrid capacitor | |
| CN112794324A (en) | High-mesoporosity lignin hierarchical pore carbon material and preparation method and application thereof | |
| CN111547723A (en) | Hemp-based hierarchical porous carbon material and preparation method and application thereof | |
| CN112265982A (en) | Preparation method of N-doped graphene/graphene nanoribbon composite aerogel | |
| CN110510595B (en) | Preparation method of N/S co-doped porous carbon for lithium-sulfur battery | |
| CN117894946A (en) | Hard carbon-graphene composite anode material for fast-charging sodium ion battery and preparation method thereof | |
| KR102357191B1 (en) | Method of Synthesizing Carbon-Based Anode Material and Interlayer for Lithium Sulfur Battery from Carbon Dioxide | |
| CN117125694A (en) | High-power asphalt-based sodium ion battery carbon negative electrode material, and preparation method and application thereof | |
| CN114380285B (en) | Carbon aerogel material with synergistic enhancement of one-dimensional biological carbon and two-dimensional biological carbon, and preparation method and application thereof | |
| CN115124020A (en) | Boron-nitrogen co-doped carbon material with hierarchical holes and preparation method and application thereof | |
| CN112670097B (en) | Preparation method of loofah sponge-based derived carbon electrode material with three-dimensional network structure | |
| CN111313020B (en) | Preparation method of sulfur-doped nitrogen-rich carbon material, electrode and application of sulfur-doped nitrogen-rich carbon material in sodium/potassium ion battery | |
| CN110690423B (en) | Heteroatom doped carbon material and preparation method and application thereof | |
| CN111554925B (en) | Preparation method of graphene doped wormcast composite material | |
| CN112201484A (en) | Two-dimensional ultrathin carbon nanosheet and preparation method and application thereof | |
| CN112429714A (en) | Preparation process of modified super-capacitor carbon | |
| CN111924842A (en) | Lotus stalk-based electrode material and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |